HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908309Generated: October 25, 2026
Potassium Carbonate → N-(6-(2-amino-3-carbamoyl-5-methylphenyl)naphthalen-2-yl)thiophene-3-carboxamide
https://huagongshe.com/reaction/908309
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-Amino-3-bromo-5-methylbenzamide | HCID 58828874 | — |
| Reactant | N-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl)thiophene-3-carboxamide | HCID 67386422 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(6-(2-amino-3-carbamoyl-5-methylphenyl)naphthalen-2-yl)thiophene-3-carboxamide | HCID 58828862 | 10% |
Reaction Steps
2-amino-3-bromo-5-methylbenzamide (31.8 mg, 0.139 mmol), N-(6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl)thiophene-3-carboxamide (122 mg, 0.370 mmol), Fibercat palladium catalyst (Johnson-Matthey, 68.2 mg), and K2CO3 (2 M in water, 0.51 ml, 1.0 mmol) were combined in a microwave reaction vessel and 1,4-dioxane (1.5 ml) was added. The reaction tube was sealed and heated in the microwave (CEM microwave) at 60 Watts and 80 C for 20 minutes. The reaction was then cooled to room temperature, diluted with water (5 ml), and extracted with EtOAc (4×10 ml). The organic extracts were combined, dried over sodium sulfate, filtered, concentrated, and purified via silica gel (Biotage instrument, 13%->50%->100% EtOAc/hexanes) to afford title compound (5.6 mg, 10%). MS (ESI pos. ion) m/z: 402 (M+H). Calc'd Exact Mass for C23H19N3O2S: 401.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017601B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-1b4f42a32f1445e5861fea74e4768f8c |
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| Source note | uspto-grants-2011_09 |
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